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Clinical Trials Volunteer Jobs (NOW HIRING)

Adecco

Clinical Trials Manager- Remote

Chapel Hill, NC · Remote

$62 - $64.73/hr

Clinical Trials Manager (CTM) Location: Remote Schedule: Full-Time | Eastern Time Zone Hours Pay ... additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit ...

Bannerhealth

$20.50 - $27.25/hr

... volunteers; registering patients; providing information on clinical trials and protocols to interested participants in a timely and helpful manner; obtaining relevant medical history on candidates by ...

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Clinical Trials Volunteer information

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$28K

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How much do clinical trials volunteer jobs pay per year?

As of Aug 22, 2026, the average yearly pay for clinical trials volunteer in the United States is $67,542.00, according to ZipRecruiter salary data. Most workers in this role earn between $53,500.00 and $78,500.00 per year, depending on experience, location, and employer.

What is a clinical trials volunteer?

A Clinical Trials Volunteer participates in research studies to help test new medical treatments, drugs, or devices. Volunteers may receive investigational treatments under strict medical supervision while contributing to advancements in healthcare. Participation is voluntary, and studies follow ethical guidelines to ensure safety. Eligibility depends on factors like age, health condition, and study requirements. Volunteers may receive compensation for their time and travel.

What can I expect during the process of participating as a clinical trials volunteer?

As a Clinical Trials Volunteer, you can expect to attend scheduled visits, provide health information, and sometimes undergo basic medical assessments or procedures, depending on the study. You'll be closely monitored by research staff who will guide you through each step and address any concerns you may have. While some trials require only a few hours of commitment, others may involve multiple visits or longer-term follow-up. Collaboration is frequent, as you'll interact with clinical coordinators, nurses, and sometimes other volunteers. This structured environment is designed to ensure both the success of the study and your comfort and safety as a participant.

What are the key skills and qualifications needed to thrive as a clinical trials volunteer, and why are they important?

To thrive as a Clinical Trials Volunteer, you should possess good general health, reliability, and a willingness to follow detailed instructions. No specific technical tools or certifications are typically required, but volunteers may interact with basic health monitoring equipment or complete electronic questionnaires as part of the trial. Dependability, effective communication, and comfort with regular check-ins or medical procedures are valued soft skills in this position. These qualities are important because they ensure the integrity of the clinical trial and the safety and well-being of both participants and research staff.

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What cities are hiring for Clinical Trials Volunteer jobs?

Cities with the most Clinical Trials Volunteer job openings:

What are the most commonly searched types of Clinical Trials jobs?

The most popular types of Clinical Trials jobs are:

What states have the most Clinical Trials Volunteer jobs?

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Clinical Trials Volunteer jobs near you
Infographic showing various Clinical Trials Volunteer job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 67% In-person, and 33% Remote job distribution, with an average salary of $67,542 per year, or $32.5 per hour.

Clinical Trials Research Nurse

University Health Partners of Hawai'i (UCERA)

Honolulu, HI • On-site

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 11 days ago

Job description

ESSENTIAL JOB DUTIES AND FUNCTIONS
  • Independently oversees education, support and conducts research using sound nursing judgement, critical thinking, and clinical knowledge and skills. Responsible for the effective and ethical conduct of oncology clinical trials. Coordinates, evaluates, and follows patients in clinical trials, which includes but is not limited to screening, identifying, enrolling and consenting patients, developing study calendars with Clinical Trial Management System team, coordinating study visits and follow-ups, and any other study-related activities. Ensures adherence to protocol requirements, and reports and documents deviations as appropriate. Performs protocol-specific clinical tasks including patient assessment, ordering tests, collecting specimens, and monitoring responses to interventions. Serves as a resource to research and clinical staff regarding protocol requirements. Reviews clinic schedules and medical records of potential clinical trials participants, matching patient characteristics with eligibility requirements of available protocols. Assists physicians and cancer care staff in coordinating laboratory tests/procedures required for pre-study testing. May dispense investigational drug under the direction of the physician, and provide patient teaching regarding administration. Maintains accurate investigational drug accountability records. Assists in collecting, processing, and preparing patient specimens for shipment as required by protocol. Assists in collecting and transmitting patient-reported information (questionnaires).
  • Provides general clinical research, as well as study-specific information to patients and research, clinical, and other organizational staff. Serves as a resource to CRAs for any study-related issues to facilitate coordination amongst various hospital/clinic departments as required by the studies.
  • Ensures validity of research results by ensuring timely, accurate and complete data documentation, reporting deviations, violations and serious adverse events. Responsible for all protocol data collection including completion of initial study forms, treatment forms and follow-up forms. Enters all patient tracking information into OnCore Clinical Trials Management System and/or other required data capture system in a timely manner. Reviews data for accuracy and submits data within time requirements, electronically if required.
  • Ensures patient safety. Monitors patients for adverse events and reports according to standard guidelines or as specified in the protocol. In collaboration with the physician, reviews patients for changes in conditions, adverse events, concomitant medications use, protocol compliance, response to study drug, and thoroughly documents all findings. Monitors patients for serious adverse events per Federal and/or sponsor guidelines, within the time parameters.
  • Develops relationships with community partners to facilitate accrual to and compliance with clinical trials. Assists in implementation of recruitment plans to identify and assess potential clinical trial participants. Identifies and develops processes to overcome barriers to clinical trial enrollment.
  • Assists in the maintenance and distribution of clinical protocols available for patient enrollment. Provides input on new studies and study continuation. Assists in reviewing availability for industry-sponsored trials and communicating opportunities with clinical research staff and affiliated oncology practitioners.
  • Attends UHCC clinical meetings and tumor boards at local hospitals. Completes feasibility forms and PowerPoint slides for UHCC meetings as needed. Assists in preparing for external audits and in developing corrective action plans as needed. Participates in quality assurance internal audits. Works with regulatory staff to develop patient consents.
  • Provides in-service training on protocol requirements to clinic staff by working closely with the PI and staff to ensure that clinical procedures are completed according to protocol. This includes preparing amendments and any changes or updates in procedures and activities, which support the protocol, and disseminating all pertinent information affecting study conduct to staff throughout the duration of the study. Prepares and organizes materials for distribution to patients and clinics.
  • Provides mentoring, education, and problem solving to research team. Advocates for clinical trials by participating in community outreach efforts to provide general clinical trials education when opportunities arise. Oversees students and/or volunteers. May mentor and train CRAs and other research support staff.
  • Acts as the team's lead authority for specific technical areas of clinical trials, such as training, continuing education, and quality control. Maintains working knowledge of oncology clinical care and research. Participates in education, instruction, and professional development as necessary to maintain job-related skills and competencies. Completes continuing medical education courses as deemed relevant and attends meetings and conferences as appropriate.
  • Provides in-service training on protocol requirements to clinic staff by working closely with the PI and staff to ensure that clinical procedures are completed according to protocol.
  • Complies with all legal requirements and company policies.
  • Maintains patient confidentiality at all times.
  • Performs all other duties as assigned.
Please see the attached job description for more information.
QUALIFICATION REQUIREMENTS
Education/Training/Experience
Minimum:
  • Bachelor's Degree from an accredited four (4) year college or university in Nursing. (Associate's Degree from an accredited community college in Nursing with at least two (2) years of professional experience in health sector may substitute for a Bachelor's Degree.)
  • Must possess a State of Hawai'i RN license
  • Must complete Collaborative Institutional Training Initiative (CITI) Human Subject training within three (3) months from date of hire.
  • Current BLS CPR Certification
  • Four years of experience as a Registered Nurse (RN) in a related clinical specialty (e.g., oncology) or clinical trials experience in oncology.
Preferred:
  • Master's Degree from an accredited college or university in Nursing.
  • Oncology Certified Nurse (OCN), Certified Clinical Research Coordinator (CCRC), or Certified Clinical Research Professional (CCRP).
  • Experience in IV access placement, venous access devices, oncology medication administration and monitoring including oral therapies, injections and infusion
Skills/Knowledge
Minimum:
  • Demonstrated knowledge in human subjects' research and International Conference on Harmonization (ICH)
  • Demonstrated knowledge in Good Clinical Practices (GCP)
  • Demonstrated knowledge in Health Insurance Portability and Accountability Act (HIPAA) training.
  • Understanding of research study designs and ethics.
  • Knowledge of and experience with computers and software programs, including word-processing, spreadsheets, and database.
  • Specialized knowledge of clinical trial protocols grouped from a specific National Cancer Institute (NCI) research base, other source, or by disease site, etc.
  • Specialized knowledge of specific cancer care sites conducting clinical trials or of job areas, such as education/training, regulatory, investigational drug accountability/storage, specimen collection/processing, database maintenance/reporting, and auditing.
  • Strong and effective written and verbal communication skills.
Preferred:
  • Working knowledge of the University of Hawai'i and UHCC policies and procedures.
BENEFITS
  • Generous time off benefits
  • 100% employee health and dental coverage and vision
  • Flexible spending plan
  • Retirement plan with up to 3% dollar-for-dollar company matching contributions
  • 100% company paid group Life/AD&D/LTD insurance
  • Employee assistance program (EAP)
  • Pet Insurance, Prepaid legal with competitive rates

UHP Hawai'i is an EEO employer.

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